Gómez-Lagunas F, Olamendi-Portugal T, Possani L D
Department of Molecular Recognition and Structural Biology, Institute of Biotechnology, Universidad Nacional Autónoma de México, Cuernavaca.
FEBS Lett. 1997 Jan 3;400(2):197-200. doi: 10.1016/s0014-5793(96)01387-7.
Here we describe the basic features of the interaction of K+ channels with Pi1, a recently described 35 amino acid scorpion toxin, which has four disulfide bridges instead of the three commonly found in all the other known scorpion toxins. We found that: (a) Pi1 blocks ShakerB from the outside with a 1:1 stoichiometry, and a Kd of 32 nM in zero external [K+]; (b) extracellular K+, Rb+ and Cs+ but not NH4+ ions strongly impede (destabilize) the block by this toxin; interestingly (c) the destabilizing binding of K+, Rb+, and Cs+ is described by a Hill coefficient n > 1; (d) external K+ is more effective than internal K+ to reduce the block by Pi1.
在此,我们描述了钾离子通道与Pi1(一种最近描述的含有35个氨基酸的蝎毒素)相互作用的基本特征,Pi1具有四个二硫键,而不是所有其他已知蝎毒素中常见的三个。我们发现:(a)Pi1以1:1的化学计量比从外部阻断ShakerB,在零外部[K+]时的解离常数Kd为32 nM;(b)细胞外的K+、Rb+和Cs+离子(但不是NH4+离子)会强烈阻碍(使不稳定)这种毒素的阻断作用;有趣的是(c)K+、Rb+和Cs+的不稳定结合由希尔系数n>1来描述;(d)外部K+比内部K+更有效地减少Pi1的阻断作用。